Thursday, January 20, 2011

New randomised controlled trial shows that CBT and GET make things worse in ME/CFS

By Núñez M, Fernández-Solà J, Nuñez E, Fernández-Huerta JM, Godás-Sieso T, Gomez-Gil E:
Health-related quality of life in patients with chronic fatigue syndrome: group cognitive behavioural therapy and graded exercise versus usual treatment. A randomised controlled trial with 1 year of follow-up. [JOURNAL ARTICLE]
Clin Rheumatol 2011 Jan 15


Chronic fatigue syndrome (CFS) produces physical and neurocognitive disability that significantly affects health-related quality of life (HRQL).

Multidisciplinary treatment combining graded exercise therapy (GET) cognitive behavioural therapy (CBT) and pharmacological treatment has shown only short-term improvements.

To compare the effects on HRQL of (1) multidisciplinary treatment combining CBT, GET, and pharmacological treatment, and (2) usual treatment (exercise counselling and pharmacological treatment) at 12 months of follow-up. Prospective, randomized controlled trial with a follow-up of 12 months after the end of treatment.

Patients consecutively diagnosed with CFS (Fukuda criteria) were randomly assigned to intervention (n = 60) or usual treatment (n = 60) groups. HRQL was assessed at baseline and 12 months by the Medical Outcomes Study Short-Form questionnaire (SF-36). Secondary outcomes included functional capacity for activities of daily living measured by the Stanford Health Assessment Questionnaire (HAQ) and comorbidities.

At baseline, the two groups were similar, except for lower SF-36 emotional role scores in the intervention group. At 12 months, the intervention did not improve HRQL scores, with worse SF-36 physical function and bodily pain scores in the intervention group. Multidisciplinary treatment was not superior to usual treatment at 12 months in terms of HRQL.

2 comments:

Creek said...

Thank you for this post.

It's all in the design of the research, isn't it? A well-designed study shows what any patient can tell you: exercise makes it worse.

Further, it's interesting when a study like the Lights' can show some of the how and why exercise induces pain and increases debility in ME.

Nicky Reiss said...

We also need to look at how the insurance companies are involved. Take a look at this:

http://www.meactionuk.org.uk/UNUMProvident_Sharpe_and_CBT.htm

Keep up the good work!

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